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多杀菌素再利用作为一种新的抗寨卡病毒药物。

Repurposing of Doramectin as a New Anti-Zika Virus Agent.

机构信息

School of Public Health, Sun Yat-sen University, Guangzhou 510080, China.

Key Laboratory of Tropical Disease Control (Sun Yat-sen University), Ministry of Education, Guangzhou 510080, China.

出版信息

Viruses. 2023 Apr 27;15(5):1068. doi: 10.3390/v15051068.

Abstract

Zika virus (ZIKV), belonging to the family and mainly transmitted by mosquitoes, causes a variety of adverse outcomes, including Guillain-Barré syndrome, microcephaly, and meningoencephalitis. However, there are no approved vaccines or drugs available for ZIKV. The discovery and research on drugs for ZIKV are still essential. In this study, we identified doramectin, an approved veterinary antiparasitic drug, as a novel anti-ZIKV agent (EC value from 0.85 μM to 3.00 μM) with low cytotoxicity (CC > 50 μM) in multiple cellular models. The expression of ZIKV proteins also decreased significantly under the treatment of doramectin. Further study showed that doramectin directly interacted with the key enzyme for ZIKV genome replication, RNA-dependent RNA polymerase (RdRp), with a stronger affinity (K = 16.9 μM), which may be related to the effect on ZIKV replication. These results suggested that doramectin might serve as a promising drug candidate for anti-ZIKV.

摘要

寨卡病毒(ZIKV)属于黄病毒科,主要通过蚊子传播,可引起多种不良后果,包括格林-巴利综合征、小头畸形和脑膜脑炎。然而,目前尚无针对 ZIKV 的批准疫苗或药物。因此,对 ZIKV 药物的发现和研究仍然至关重要。在这项研究中,我们发现多拉菌素是一种已批准的兽用驱虫药,它是一种新型抗 ZIKV 药物(EC 值为 0.85 μM 至 3.00 μM),在多种细胞模型中具有低细胞毒性(CC > 50 μM)。多拉菌素处理后,ZIKV 蛋白的表达也显著下降。进一步研究表明,多拉菌素可直接与 ZIKV 基因组复制的关键酶,即 RNA 依赖性 RNA 聚合酶(RdRp)相互作用,亲和力较强(K = 16.9 μM),这可能与其对 ZIKV 复制的作用有关。这些结果表明多拉菌素可能是一种有前途的抗 ZIKV 药物候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df4a/10221537/a4e29541fdf4/viruses-15-01068-g001.jpg

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